2-(benzylamino)-5-(4-(2,6-dichlorobenzyloxy)phenyl)thiophene-3-carboxylic acid

Base Information

Chemical Name:2-(benzylamino)-5-(4-(2,6-dichlorobenzyloxy)phenyl)thiophene-3-carboxylic acid
CAS No.:1334931-67-7
Molecular Formula:C₂₅H₁₉Cl₂NO₃S
Molecular Weight:484.403
Hs Code.:

Synonyms:2-(benzylamino)-5-(4-(2,6-dichlorobenzyloxy)phenyl)thiophene-3-carboxylic acid

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Chemical Property of 2-(benzylamino)-5-(4-(2,6-dichlorobenzyloxy)phenyl)thiophene-3-carboxylic acid

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Technology Process of 2-(benzylamino)-5-(4-(2,6-dichlorobenzyloxy)phenyl)thiophene-3-carboxylic acid

There total 6 articles about 2-(benzylamino)-5-(4-(2,6-dichlorobenzyloxy)phenyl)thiophene-3-carboxylic acid which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 60.0%

: 1334931-23-5
ethyl 2-(benzylamino)-5-(4-(2,6-dichlorobenzyloxy)phenyl)thiophene-3-carboxylate

: 1334931-67-7
2-(benzylamino)-5-(4-(2,6-dichlorobenzyloxy)phenyl)thiophene-3-carboxylic acid

Guidance literature:: ethyl 2-(benzylamino)-5-(4-(2,6-dichlorobenzyloxy)phenyl)thiophene-3-carboxylate; With sodium hydroxide; In ethanol; for 2h; Reflux;

With hydrogenchloride; In water; pH=4 - 5;
DOI:10.1016/j.ejmech.2011.05.018

Reference yield:

: 1334930-83-4
2-(4-(2,6-dichlorobenzyloxy)phenyl)ethanol

: 1334931-67-7
2-(benzylamino)-5-(4-(2,6-dichlorobenzyloxy)phenyl)thiophene-3-carboxylic acid

Guidance literature:: Multi-step reaction with 4 steps

1.1: sodium bromite trihydrate; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; sodium hydrogencarbonate / dichloromethane; water / 0.5 h / 0 - 20 °C / pH 8.6

2.1: sulfur; triethylamine / ethanol / 60 °C

3.1: potassium carbonate; potassium iodide / N,N-dimethyl-formamide / 24.5 h / 20 - 60 °C

4.1: sodium hydroxide / ethanol / 2 h / Reflux

4.2: pH 4 - 5

With 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; sodium bromite trihydrate; sodium hydrogencarbonate; potassium carbonate; sulfur; triethylamine; potassium iodide; sodium hydroxide; In ethanol; dichloromethane; water; N,N-dimethyl-formamide;
DOI:10.1016/j.ejmech.2011.05.018

Reference yield:

: 1334930-94-7
ethyl 5-(4-(2,6-dichlorobenzyloxy)phenyl)-2-aminothiophene-3-carboxylate

: 1334931-67-7
2-(benzylamino)-5-(4-(2,6-dichlorobenzyloxy)phenyl)thiophene-3-carboxylic acid

Guidance literature:: Multi-step reaction with 2 steps

1.1: potassium carbonate; potassium iodide / N,N-dimethyl-formamide / 24.5 h / 20 - 60 °C

2.1: sodium hydroxide / ethanol / 2 h / Reflux

2.2: pH 4 - 5

With potassium carbonate; potassium iodide; sodium hydroxide; In ethanol; N,N-dimethyl-formamide;
DOI:10.1016/j.ejmech.2011.05.018